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Monteiro-Soares, M., Boyko, E

The FDA describes a facility where drug products intended to be sterile were produced in environments that may not have provided adequate contamination protection, where products that failed sterility and potency testing were released and distributed, where out-of-specification investigation procedures were not followed in a single documented case out of 23 reviewed, and where patients were not notified when the drugs they received were found to be subpotent or failed sterility testing

The mechanism most safety reasoning is built on is therefore reported as proposed, in papers later retracted which widens the uncertainty around both how Dihexa acts and what its long-term effects might be

Pattern and Consequences of Krathom (Mitragyna Speciosa Korth.) Use Among Male Villagers in Southern Thailand: A Qualitative Study